
[Federal Register: March 29, 2010 (Volume 75, Number 59)]
[Proposed Rules]               
[Page 15387-15388]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr29mr10-18]                         

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Parts 510, 514, and 558

[Docket No. FDA-2010-N-0155]

 
Veterinary Feed Directive

AGENCY: Food and Drug Administration, HHS.

ACTION: Advance notice of proposed rulemaking.

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SUMMARY: The Food and Drug Administration (FDA or the agency) is 
announcing an advance notice of proposed rulemaking (ANPRM) to solicit 
comments from the public regarding potential changes to its current 
regulation relating to veterinary feed directive (VFD) drugs. FDA's VFD 
regulation, which became effective on January 8, 2001, established 
requirements relating to the distribution and use of VFD drugs and 
animal feeds containing such drugs. FDA is undertaking a review of 
these requirements in an effort to identify possible changes to improve 
efficiency. Therefore, the agency is requesting public comment on all 
aspects of the VFD regulation, particularly suggestions relating to 
improving efficiency. This information may be used to help draft a 
proposed rule in the near future.

DATES: Submit electronic or written comments by June 28, 2010.

ADDRESSES: You may submit comments, identified by Docket No. FDA-2010-
N-0155, by any of the following methods:
Electronic Submissions
    Submit electronic comments in the following way:
     Federal eRulemaking Portal: http://www.regulations.gov. 
Follow the instructions for submitting comments.
Written Submissions
    Submit written submissions in the following ways:
     FAX: 301-827-6870.
     Mail/Hand delivery/Courier (for paper, disk, or CD-ROM 
submissions): Division of Dockets Management (HFA-305), Food and Drug 
Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.
    Instructions: All submissions received must include the agency name 
and docket number for this rulemaking. All comments received may be 
posted without change to http://www.regulations.gov, including any 
personal information provided. For additional information on submitting 
comments, see the ``Comments'' heading of the SUPPLEMENTARY INFORMATION 
section of this document.
    Docket: For access to the docket to read background documents or 
comments received, go to http://www.regulations.gov and insert the 
docket number, found in brackets in the heading of this document, into 
the ``Search'' box and follow the prompts and/or go to the Division of 
Dockets Management, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.

FOR FURTHER INFORMATION CONTACT: Neal Bataller, Center for Veterinary 
Medicine (HFV-230), Food and Drug Administration, 7500 Standish Pl., 
Rockville, MD 20855, 240-276-9201, e-mail: Neal.Bataller@fda.hhs.gov.

SUPPLEMENTARY INFORMATION:

I. Background

    Before 1996, two options existed for regulating the distribution of 
animal drugs, including drugs in animal feed: (1) Over-the-counter 
(OTC) and (2) prescription. In 1996, Congress passed and the President 
signed into law the Animal Drug Availability Act (ADAA) (Public Law 
104-250), to facilitate the approval and marketing of new animal drugs 
and medicated feeds. As part of the ADAA, Congress determined that 
certain new animal drugs should be approved for use in animal feed but 
only if these medicated feeds were administered under a veterinarian's 
order and professional supervision. Therefore, the ADAA created a new 
category of products called veterinary feed directive drugs (or VFD 
drugs). VFD drugs are new animal drugs intended for use in or on animal 
feed which are limited to use under the professional supervision of a 
licensed veterinarian in the course of the veterinarian's professional 
practice.
    In the Federal Register of December 8, 2000 (65 FR 76924), FDA 
issued a final rule amending the new animal drug regulations to 
implement the VFD-related provisions of the ADAA. FDA reaffirmed that 
certain new animal drugs should be approved for use in animal feed only 
if these medicated feeds are administered under a veterinarian's order 
and professional supervision. Veterinarian oversight is important for 
assuring the safe and appropriate use of certain new animal drugs. For 
example, safety concerns relating to the difficulty of disease 
diagnosis, drug toxicity, drug residues, antimicrobial resistance, or 
other reasons may dictate that the use of a medicated feed be limited 
to use by order and under the supervision of a licensed veterinarian.
    It has been 9 years since FDA began implementing the final rule 
regulating VFDs. Although, currently there are few approved VFD animal 
drug products, FDA has received a number of informal general comments 
that characterize the current VFD process as being overly burdensome. 
In addition, there are concerns that the process in its current form 
will become particularly problematic to administer in the future as the 
number of approved VFD animal drugs increases. When veterinary 
oversight of a medicated feed is determined to be necessary, it is 
critically important that such oversight be facilitated through an 
efficient VFD process. In response to these concerns, the agency is 
undertaking a review of the VFD regulations to determine whether 
changes are warranted to improve the program's efficiency.

II. Agency Request for Comments

    The purpose of this document is to solicit public comment on 
whether such efficiency improvements are needed and, if so, on possible 
revisions to the VFD regulations. Such comments are welcome on all 
aspects of the VFD regulation. To facilitate FDA's review of

[[Page 15388]]

submitted comments, please organize your comments based on the major 
categories of requirements included in the current VFD regulation at 21 
CFR 558.6. These categories of requirements are listed following this 
paragraph. (See A through F.) If your comment addresses an issue 
outside of one of these categories, please categorize your comment as 
G. ``Other:''
    A. Conditions that must be met by veterinarians issuing a VFD;
    B. What veterinarians must do with a VFD (e.g., disposition of 
original VFD and copies);
    C. Records that must be kept related to the VFDs;
    D. Notification requirements for distributors of animal feeds 
containing a VFD drug;
    E. Additional recordkeeping requirements that apply to 
distributors;
    F. Cautionary statements required for VFD drugs and animal feeds 
containing VFD drugs; and
    G. Other.

III. Comments

    Interested persons may submit to the Division of Dockets Management 
(see ADDRESSES) electronic or written comments regarding this document. 
Submit a single copy of electronic comments or two paper copies of any 
mailed comments, except that individuals may submit one paper copy. 
Comments are to be identified with the docket number found in brackets 
in the heading of this document. Received comments may be seen in the 
Division of Dockets Management between 9 a.m. and 4 p.m., Monday 
through Friday.

    Dated: March 24, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010-6872 Filed 3-26-10; 8:45 am]
BILLING CODE 4160-01-S

